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BDBM606639

E3L030024
Internal ID: BDB030024
Activity data available Local docking-ready structure
Dock with Q92794
Structure
/e3_file/ligand_db/generated/BDB030024/BDB030024.sdf
Basic Properties
Compound ID
E3L030024
Internal ID
BDB030024
Molecular formula
C19H23ClFN5O4S
Molecular weight
471.942000
Exact mass
471.114331
XLogP
1.5582
TPSA
113.4000
HBA / HBD
5 / 2
Rotatable bonds
6
Heavy atoms / rings
31 / 3
Activity summary
IC50 unknown 30000.00000000 nM
1 activity record(s) imported
InChIKey
HJEKCMCHYIIJLT-SMDDNHRTSA-N
SMILES
CC(=O)N1C[C@H](CS(=O)(=O)NNC(=O)c2cc(-c3cn(C)cn3)cc(Cl)c2F)[C@@H](C)C1
Aliases
BDBM606639 (preferred) N'-[[(3R,4R)-1-acetyl-4-methylpyrrolidin-3-yl]methylsulfonyl]-3-chloro-2-fluoro-5-(1-methylimidazol-4-yl)benzohydrazide (source_name) BDBM606639 (source_id)
E3 Relation
E3 UniProt Gene / protein Relation type Ligand role Direct Functional Docking Source Evidence
Q92794 KAT6A;MOZ;MYST3;RUNXBP2;ZNF220
Histone acetyltransferase KAT6A
reported_binder bindingdb_reported Yes No low BindingDB:BDBM606639 medium
; target=Histone acetyltransferase KAT6A
Sources and Literature
Source Source ID Source URL Download URL DOI / PMID
BindingDB BDBM606639 Open - 10.7270/Q28G8QTD
PubChem CID168474387 Open -
Structure Files
Kind Format Status Docking use File / link Preparation note
canonical_2d SMILES raw Docking-ready CC(=O)N1C[C@H](CS(=O)(=O)NNC(=O)c2cc(-c3cn(C)cn3)cc(Cl)c2F)[C@@H](C)C1 keep_bindingdb_unique
generated_3d SDF prepared Docking-ready public/e3_file/ligand_db/generated/BDB030024/BDB030024.sdf Generated from canonical SMILES
generated_3d MOL2 prepared Docking-ready public/e3_file/ligand_db/generated/BDB030024/BDB030024.mol2 Generated from canonical SMILES
docking_ready PDBQT prepared Docking-ready public/e3_file/ligand_db/generated/BDB030024/BDB030024.pdbqt Generated from canonical SMILES
image PNG prepared Reference public/e3_file/ligand_db/generated/BDB030024/BDB030024.png Generated from canonical SMILES
image SVG prepared Reference public/e3_file/ligand_db/generated/BDB030024/BDB030024.svg Generated from canonical SMILES
Activity
Target Source Assay Result Potency Literature Records
Histone acetyltransferase KAT6A
Q92794
E3 ligase component
BindingDB:BDBM606639 IC50 30000 nM Low DOI: 10.7270/Q28G8QTD 1